15

This is our test site on Maui, flying across the sky.

An approval of a clinical trial should not be granted until an independent ethics committee has issued a favourable opinion.

The number of scientific advice given in 2002 remains stable Average number of days for scientific advice procedures

In Japan, it is very difficult to find a suitable test site to perform this test.

The treaty was signed on 8 September 2006 at Semipalatinsk Test Site, Kazakhstan, and is also known as Treaty of Semipalatinsk, Treaty of Semei, or Treaty of Semey.

Test procedure

Test apparatus

Test speed

Test surfaces

Test surfaces

TRIAL PERIOD

the Member may, as appropriate, issue the notification or guidance based on risk

With reference to the above, the Government of the Republic of Moldova has the honour to notify the Preparatory Committee that the Republic of Moldova designates the following provisions contained in Section I of the Agreement (annexed to the above mentioned Ministerial Decision) as Category A commitments, which will be implemented upon entry into force of the Agreement

Spectacle lenses of glass

Disposable cameras

Toothed wheels, chain sprockets and other transmission elements presented separately

Test Method

Test sequence

Testing procedures

Test methodology

TEST PROCEDURE

Testing requirements

Test procedure

Test procedure

Test Procedure

Test procedure

Test sequence

Test mixture

Test mixture

Test surfaces

(c) Test procedure

The Contracting Parties which have notified their disagreement, or their intention not to accept the exemption approval immediately, with the authorisation by the Administrative Committee may at a later date accept the exemption approval by notifying the Executive Secretary of the United Nations Economic Commission for Europe of their decision.

When the authorisation for granting the exemption approval is adopted, the Executive Secretary of the United Nations Economic Commission for Europe shall, as soon as possible, notify the Contracting Parties applying the concerned UN Regulation about this adoption.

Test documentation

Test method 9

TEST REPORT

Equivalent test method

ENDURANCE TEST PROGRAMME

Equivalent test methods

Maximum power at the test speed under test conditions (see Annex VII, Appendix 1)

Following the feasibility study, a prototype, which was not designed for commercial production but only for testing purposes, was developed and constructed on the premises of Magog (installation 1).

The positions tested by the laboratories shall be indicated in the test report.

The duration of therapy should be guided by the severity, site of the infection, and the patient s clinical response.

all SUSARs occurring in that clinical trial, irrespective of whether the SUSAR has occurred at a trial site in a Member State or third country concerned and